Canonical Allele Identifier: CA369940798

Gene: VIPR2

Linked Data

• MyVariant Identifiers: chr7:g.158826989A>C (hg19) ; chr7:g.159034298A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.159034298A>C , CM000669.2:g.159034298A>C	GRCh38
NC_000007.13:g.158826989A>C , CM000669.1:g.158826989A>C	GRCh37
NC_000007.12:g.158519750A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262178.7:c.886T>G MANE Select	ENSP00000262178.2:p.Phe296Val
ENST00000262178.6:c.886T>G	ENSP00000262178.2:p.Phe296Val
ENST00000377633.7:c.838T>G	ENSP00000366860.3:p.Phe280Val
ENST00000402066.5:c.1309T>G	ENSP00000384497.1:p.Phe437Val
NM_001304522.1:c.646T>G	NP_001291451.1:p.Phe216Val
NM_001308259.1:c.838T>G	NP_001295188.1:p.Phe280Val
NM_003382.4:c.886T>G	NP_003373.2:p.Phe296Val
NR_130758.1:n.1072T>G
XM_005249561.2:c.961T>G	XP_005249618.1:p.Phe321Val
XM_006716107.1:c.886T>G	XP_006716170.1:p.Phe296Val
XM_006716108.2:c.697T>G	XP_006716171.1:p.Phe233Val
XM_011516550.1:c.838T>G	XP_011514852.1:p.Phe280Val
XM_011516552.1:c.472T>G	XP_011514854.1:p.Phe158Val
XM_005249561.3:c.961T>G	XP_005249618.1:p.Phe321Val
XM_006716107.2:c.886T>G	XP_006716170.1:p.Phe296Val
XM_006716108.3:c.697T>G	XP_006716171.1:p.Phe233Val
XM_011516550.2:c.838T>G	XP_011514852.1:p.Phe280Val
XM_017012580.1:c.472T>G	XP_016868069.1:p.Phe158Val
XM_024446914.1:c.961T>G	XP_024302682.1:p.Phe321Val
XM_024446915.1:c.961T>G	XP_024302683.1:p.Phe321Val
XM_024446916.1:c.886T>G	XP_024302684.1:p.Phe296Val
XM_024446917.1:c.697T>G	XP_024302685.1:p.Phe233Val
XM_024446918.1:c.472T>G	XP_024302686.1:p.Phe158Val
NM_003382.5:c.886T>G MANE Select	NP_003373.2:p.Phe296Val
NM_001304522.2:c.646T>G	NP_001291451.1:p.Phe216Val
NR_130758.2:n.982T>G